warnings
Warnings Warnings Flammable . Keep away from heat or open flame. When using this product • Use glove with application hand or always wash application hand immediately after application For external use only
NUMSTAT Antiseptic and Pain Relieving Prep Pad
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- NUMSTAT Antiseptic and Pain Relieving Prep Pad
- Generic name
- ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD
- Manufacturer
- Spectra Medical Devices, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 07d20040-9dd9-0aba-e063-6294a90ab7cf
- SPL ID
- 0ceeef4e-90fe-d542-e063-6394a90abc8d
- Version
- 2
- Effective date
- 2023-12-20
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:15:13
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M003 | openfda.application_number | |
| brand name | NUMSTAT Antiseptic and Pain Relieving Prep Pad | openfda.brand_name | |
| generic name | ALCOHOL, MENTHOL, AND BENZOCAINE PREP PAD | openfda.generic_name | |
| manufacturer name | Spectra Medical Devices, LLC | openfda.manufacturer_name | |
| ndc | package | 65282-1815-2 | openfda.package_ndc |
| ndc | package | 65282-1815-1 | openfda.package_ndc |
| ndc | product | 65282-1815 | openfda.product_ndc |
| ndc11 | package | 65282181501 | derived:openfda.package_ndc |
| ndc11 | package | 65282181502 | derived:openfda.package_ndc |
| rxcui | 2667820 | openfda.rxcui | |
| rxcui | 2667826 | openfda.rxcui | |
| spl id | 0ceeef4e-90fe-d542-e063-6394a90abc8d | id | |
| spl set id | 07d20040-9dd9-0aba-e063-6294a90ab7cf | set_id | |
| unii | U3RSY48JW5 | openfda.unii | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | ND2M416302 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.